(1R,2S,5S,6R) - 3 - aza - 3 - benzyl - 6 - Methoxycarbonylbicyclohexyl - 2 - Methanol
- Product Code: 36217
CAS:
220623-23-4
| Molecular Weight: | 261.32 g./mol | Molecular Formula: | C₁₅H₁₉NO₃ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its unique bicyclic structure and functional groups. Its stereochemistry and functional moieties make it a valuable intermediate in the synthesis of complex molecules, particularly in the development of pharmaceuticals. The presence of the methoxycarbonyl group and benzyl-substituted nitrogen allows for further chemical modifications, enabling the creation of compounds with potential biological activity. It is often employed in the design of enzyme inhibitors or receptor modulators, where its rigid bicyclic framework can contribute to precise molecular interactions. Additionally, the compound's chiral centers make it useful in asymmetric synthesis, aiding in the production of enantiomerically pure drugs. Its applications are particularly relevant in the development of central nervous system (CNS) drugs, where such structures are often explored for their ability to cross the blood-brain barrier.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿9,000.00 |
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(1R,2S,5S,6R) - 3 - aza - 3 - benzyl - 6 - Methoxycarbonylbicyclohexyl - 2 - Methanol
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its unique bicyclic structure and functional groups. Its stereochemistry and functional moieties make it a valuable intermediate in the synthesis of complex molecules, particularly in the development of pharmaceuticals. The presence of the methoxycarbonyl group and benzyl-substituted nitrogen allows for further chemical modifications, enabling the creation of compounds with potential biological activity. It is often employed in the design of enzyme inhibitors or receptor modulators, where its rigid bicyclic framework can contribute to precise molecular interactions. Additionally, the compound's chiral centers make it useful in asymmetric synthesis, aiding in the production of enantiomerically pure drugs. Its applications are particularly relevant in the development of central nervous system (CNS) drugs, where such structures are often explored for their ability to cross the blood-brain barrier.
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